"PreventionGenetics, part of Exact Sciences"[submitter] AND "TBX20"[ge - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2450715	NM_001077653.2(TBX20):c.1334C>T (p.Pro445Leu)	TBX20 (P445L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2632965	NM_001077653.2(TBX20):c.1285C>A (p.Pro429Thr)	TBX20 (P429T)	Single nucleotide variant (missense variant)	TBX20-related disorder	GUncertain significance
Select item 3047068	NM_001077653.2(TBX20):c.953_955delinsAGA (p.Gly318_Gly319delinsGluArg)	TBX20	Indel (missense variant)	TBX20-related disorder	GUncertain significance
Select item 1677551	NM_001077653.2(TBX20):c.569C>A (p.Pro190His)	TBX20 (P190H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 2628774	NM_001077653.2(TBX20):c.551A>G (p.Tyr184Cys)	TBX20 (Y184C)	Single nucleotide variant (missense variant)	TBX20-related disorder	GUncertain significance
Select item 1505333	NM_001077653.2(TBX20):c.549C>G (p.Leu183=)	TBX20	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 518497	NM_001077653.2(TBX20):c.501C>T (p.Ser167=)	TBX20	Single nucleotide variant (synonymous variant)	TBX20-related disorder +3 more	GBenign/Likely benign
Select item 1550222	NM_001077653.2(TBX20):c.381-21CT[9]	TBX20	Microsatellite (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2044032	NM_001077653.2(TBX20):c.381-21CT[6]	TBX20	Microsatellite (intron variant)	TBX20-related disorder +1 more	GLikely benign
Select item 1651654	NM_001077653.2(TBX20):c.381-21CT[7]	TBX20	Microsatellite (intron variant)	Cardiovascular phenotype +2 more	GBenign/Likely benign
Select item 519138	NM_001077653.2(TBX20):c.297A>G (p.Lys99=)	TBX20	Single nucleotide variant (synonymous variant)	TBX20-related disorder +3 more	GBenign/Likely benign
Select item 2631090	NM_001077653.2(TBX20):c.271A>T (p.Ile91Phe)	TBX20 (I91F)	Single nucleotide variant (missense variant)	TBX20-related disorder	GUncertain significance
Select item 1536048	NM_001077653.2(TBX20):c.147G>A (p.Ser49=)	TBX20	Single nucleotide variant (synonymous variant)	TBX20-related disorder +1 more	GLikely benign
Select item 1760351	NM_001077653.2(TBX20):c.124C>T (p.Leu42=)	TBX20	Single nucleotide variant (synonymous variant)	TBX20-related disorder +2 more	GLikely benign